Aromatic esters of macrolidic and lincosamidic antibiotics and pharmaceutical and cosmetic compositions containing them

ABSTRACT

Aromatic esters of macrolidic and lincosamidic antibiotics are employed in the treatment of acne.

The present invention relates to aromatic esters of macrolidic and lincosamidic antibiotics, to a process for their preparation and to pharmaceutical and cosmetic compositions containing them for the treatment of various dermatoses, and principally in the treatment of acne.

More particularly, the esters in accordance with the present invention, are intended for the treatment of dermatoses, infectious or not.

In the treatment of acne, erythromycin among the macrolides as well as clindamycin among the lincosamides have been more particularly recommended, but their use requires (particularly for erythromycin) relatively high concentrations so as to obtain a satisfactory result.

Moreover, treatment with these antibiotics has proved, in certain cases, less effective, in the measure where certain strains of propionibacterium acnes have exhibited a progressive resistance in their regard.

The topical application of clindamycin and more particularly erythromycin collides, besides, with a problem of penetration through the corneum stratum limiting from this fact their efficacy.

The esters of antibiotics in accordance with the invention provide a satisfactory solution to the problem raised by the use of these antibiotics in the treatment of acne, in the measure where it is established that these esters have an activity on propionibacterium acnes the main germ responsible for the inflammation phenomena of the skin.

The aromatic esters in accordance with the invention have from the fact of their structure a pronounced lipophilic character which facilitates a better penetration across the epidermis.

The new esters in accordance with the invention are well tolerated by the skin and are revealed to be much less toxic when taken orally than the antibiotic/acid combination.

Besides, they exhibit, with respect to known esters, the advantage of possessing a potential comedolytic activity due to the corresponding acid chain, which confers to these esters an image of a "prodrug".

The state of the art relative to esters of macrolides is represented principally by French patent No. 85.07287 (2.582.000) which relates to poly unsaturated fatty esters of erythromycin A such as the linoleate, and the linolenate of erythromycin A.

The state of the art relative to esters of lincosamides is represented principally by German patent No. 2.017.003 which describes the preparation of esters of lincomycin and clindamycin whose acyl chain has between 1 and 18 carbon atoms.

The present invention relates to, as a new industrial product, aromatic esters of macrolides or lincosamides, said esters having the following general formula: ##STR1## wherein

R represents a macrolide or lincosamide radical,

Y represents CH or nitrogen atom,

when Y represents CH, X represents a vinylene (--CH═CH--) radical, an oxygen atom, a sulfur atom or NR₁ wherein R₁ is hydrogen or methyl,

when Y represents a nitrogen atom, X represents a sulfur atom, an oxygen atom or NH,

Ar represents an aromatic radical having one of the following formulas ##STR2## wherein

n is 0 or 1,

R₂ and R₃ represent hydrogen, linear or branched alkyl having 1-15 carbon atoms or cycloalkyl having 5-10 carbon atoms, and

Z is an oxygen atom or a sulfur atom, and mixtures and salts of said esters.

Representative cycloalkyl radicals having 5-10 carbon atoms include cyclopentyl, cyclohexyl, 1-methyl cyclohexyl and 1-adamantyl.

Representative macrolides include erythromycin A, roxithromycin, oleandomycin, josamycin and spiramycins I, II and III.

Representative lincosamides include lincomycin and clindamycin.

A--The esters of erythromycin A and roxythromycin can be represented by the formula ##STR3## wherein

R'₁ represents O (erythromycin A) or N˜O--CH₂ --O--CH₂ --CH₂ --O--CH₃ (roxythromycin), and

R' represents the following acyl radical: ##STR4## wherein

Ar, X and Y have the same meanings given above.

These esters, of erythromycin A and roxithromycin are those in position 2'.

B--The esters of oleandomycin can be represented by the following formula: ##STR5## wherein

R'₂ or R'₃ represents R' or hydrogen with the proviso that at least one of R'₂ and R'₃ represents R', and

R' has the same meaning given above.

These esters are also those in position 2' and/or 4", but they can be provided in the form of a mixture.

C--The esters of josamycin can be represented by the following formula: ##STR6## wherein

R'₂ or R'₃ represents R' or hydrogen with the proviso that at least one of R'₂ and R'₃ represents R', and R' has the same meaning given above.

These esters are those in position 9 and/or 2', but they can be provided in the form of a mixture.

D--The esters of spiramycins can be represented by the following formula: ##STR7## wherein

R'₂ and R'₃ represents R' or hydrogen with the proviso that at least one of R'₂ and R'₃ represents R' and R' has the same meaning given above and R" represents hydrogen (spiramycin I), acetyl (spiramycin II) or propionyl (spiramycin III).

These esters of spiramycin (I), (II) and (III) are those in position 2' and/or 4" and they can be provided in the form of a mixture.

E--The esters of lincomycin and clindamycin can be represented, respectively, by the following formulas (VI) and (VII): ##STR8## wherein

R' has the same meaning given above.

The esters of lincomycin (VI) and clindamycin (VII) are preferably those in position 3. However, they can be provided in the form of mixtures with the esters in position 2, 4 and 7 of lincomycin and with esters in position 2 and 4 of clindamycin.

Representative aromatic esters of antibiotics of formula (I) include the following:

2'-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]erythromycin A,

3-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]clindamycin,

2'-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]roxithromycin,

9-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]josamycin and its 2' position isomer,

2'-O-[6-(3-tert. butyl phenyl)-2-naphthalene carbonyl]erythromycin A,

2'-O-[6-[3-(1,1-dimethyl decyl)-4-methoxy phenyl]-2-naphthalene carbonyl]roxithromycin,

9-O-[6-[3-(1-adamantyl)-4-hexyloxy phenyl]-2-naphthalene carbonyl]josamycin and its 2' position isomer,

2'-O-[6-[3-(1-adamantyl)-4-decyloxy phenyl]-2-naphthalene carbonyl]spiramycin (I), (II) and (III),

2'-O-[6-[3-(1-adamantyl)-4-hydroxy phenyl]-2-naphthalene carbonyl]spiramycin (I}, (II) and (III),

2'-O-[6-[4-(1-adamantylthio) phenyl]-2-naphthalene carbonyl]erythromycin A,

3-O-[6-(3-tert. butyl-4-methoxy phenyl)-2-naphthalene carbonyl]lincomycin,

3-O-[2-[3-(1-adamantyl)-4-methoxy phenyl]-5-benzimidazole carbonyl]clindamycin,

2'-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzothiazole carbonyl]erythromycin A,

2'-O-[2-[3-1-adamantyl)-4-decyloxy phenyl]-6-benzoxazole carbonyl]roxithromycin,

9-O-[2-[3-(1-adamantyl)-4-methoxy phenyl]-6-benzo[b]furan carbonyl]josamycin and its 2' position isomer,

2'-O-[2-[3-(1-adamantyl)-4-methoxy phenyl]-6-benzo[b]thiophene carbonyl]erythromycin A,

2'-O-[2-(3-tert. butyl-4-methoxy phenyl)-6-benzo [b]furan carbonyl]oleandomycin,

2'-O-[2-[3-(1,1-dimethyl decyl)-4-methoxy phenyl]-6]benzo[b]furan-carbonyl] spiramycin (I), (II) and (III),

2'-O-[1-methyl-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-indole carbonyl] spiramycin (I), (II) and (III),

2'-O-[2-(4-tert. butyl phenyl)-6-benzimidazole carbonyl]erythromycin A,

3-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzimidazole carbonyl]lincomycin,

2'-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzoxazole carbonyl]roxithromycin,

2'-O-[2-[3-(1-adamantyl)-4-methoxy phenyl]-6-benzoxazole carbonyl]erythromycin A,

9-O-[2-(4-tert. butyl phenyl)-6-benzo [b]thiophene carbonyl]josamycin and its 2' position isomer,

3-O-[2-(4-tert. butyl phenyl)-6-benzo [b]furan carbonyl]lincomycin,

2'-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzo [b]furan carbonyl]oleandomycin,

2'-O-[2-(4-tert. butyl phenyl)-6-indole carbonyl]erythromycin A,

3-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)6-indole carbonyl]lincomycin,

2'-O-[2-(5,6,7,8-tetrahydro-5,5 8,8-tetramethyl-2-naphthyl)6-benzo [b]thiophene carbonyl]roxithromycin,

3-O-[6-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)2-naphthalene carbonyl]clindamycin, and

9-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)6-benzoxazole carbonyl]josamycin.

The present invention also relates to a process for preparing these aromatic esters.

Various procedures for esterification can be employed, but preferably this esterification is carried out in an anhydrous organic solvent medium, preferably in tetrahydrofuran alone or in mixture with another organic solvent such as pyridine, by reacting an excess of mixed anhydride of the formula: ##STR9## wherein

Ar, X and Y have the same meanings given above,

the said anhydride being prepared in situ, (for example starting with ethyl chloroformate and the corresponding acid) with a macrolide or lincosamide in base form, in the presence of an organic or mineral base such as pyridine and/or sodium bicarbonate and/or triethylamine.

This method with mixed anhydride permits to obtain preferentially esters in position 2' of macrolides and/or in position 9 principally for josamycin and/or in position 4" principally for the spiramycins and the esters in position 3 of lincosamides in good yield conditions.

The other procedures of esterification principally of lincomycin and clindamycin by the method using imidazolides of corresponding acids in an anhydrous solvent such as N,N-dimethylformamide in the presence of a base such as sodium or potassium tert. butylate lead to a mixture of esters of these antibiotics.

The present invention also relates to pharmaceutical compositions that can be administered topically, orally, parenterally or rectally as well as to cosmetic compositions for the treatment of various dermatoses, principally acne, these compositions being provided in anhydrous form and containing at least one ester in accordance with the invention, such as defined above, in an amount ranging from 0.001 to 10 weight percent, but preferably from 0.01 to 1 weight percent, based on the total weight of the composition.

For the preparation of compositions, according to the invention, containing as the active component, at least one ester according to the invention such as defined above, there can be employed vehicles and adjuvants described in the literature for pharmaceuticals, cosmetics and related fields.

For the preparation of solutions, there can be employed, for example, an acceptable organic solvent from a physiologic view point.

The acceptable organic solvent is selected principally from the group consisting of acetone, isopropyl alcohol, 1, triglycerides of fatty acids, C₁ -C₄ alkyl esters of short chain acids, polytetrahydrofuran ethers and silicones such as cyclomethicones and mixtures thereof.

The compositions according to the invention can also include a thickening agent such as a cellulose derivative in an amount ranging from 0.5 to 20 weight percent based on the total weight of the composition.

The compositions according to the invention can also contain in combination with at least one ester according to the invention, at least one other known anti-acne agent.

If necessary, a conventional adjuvant selected from the group consisting of antioxidants, preservatives, perfumes and dyes can be added.

Representative useful antioxidants include, for instance, t-butylhydroxy quinone, butylhydroxy anisole, butylhydroxy toluene and α-tocopherol and its derivatives.

The pharmacologic and galenic transformations of the compounds of the present invention are effected in a known manner.

The galenic forms can be, for topical applications, creams, milks, gels, more or less thick lotions, lotion-impregnated pads, pomades, sticks or even aerosol formulations provided in the form of sprays or foams.

The compositions for oral administration can be provided in the form of tablets, gelules, lozenges, syrups, suspensions, emulsions, powders, granules or solutions.

The compositions can also be provided in the form of suppositories.

The treatment of acne using the topical compositions of the invention comprises applying, two or three times each day, a sufficient amount on the areas of the skin being treated and this for a period of time ranging from 6 to 30 weeks and preferably from 12 to 24 weeks.

The compositions according to the invention can also be used as a preventative, i.e. on the areas of the skin susceptible of being attacked by acne.

There are now given, as an illustration, several examples of the preparation of aromatic esters of antibiotics in accordance with the invention as well as several examples of pharmaceutical or cosmetic compositions for the treatment of dermatoses, principally of acne.

EXAMPLE 1 Preparation of 2'-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]erythromycin A

In a round bottom flask, under an inert atmosphere, there are dissolved 6.8 g (16.6 mmoles) of 6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthoic acid in 35 ml of anhydrous tetrahydrofuran; the reaction mixture is cooled to 0° C., and there are then added 2.3 ml of anhydrous pyridine and 1.6 ml (16.6 mmoles) of ethyl chloroformate. The solution is stirred for 5 minutes and there are added 20ml of anhydrous pyridine, then 4.9 g (6.7 mmoles) of erythromycin A previously dissolved in 150 ml of tetrahydrofuran. The reaction mixture is stirred for 10 hours, and the temperature is permitted to return to ambient temperature (chromatography on thin layer silica gel: methylene chloride (90)/methanol (10)). The solution is poured into 60 ml of water, and then extracted with ethyl acetate. The organic phase is dried on magnesium sulfate, filtered, and then concentrated under a partial vacuum. The crude product thus obtained is chromatographed on a silica gel column (HPLC) by using as the eluant: ethyl acetate (7)/hexane (3) to result in the isolation of 4.2 g (55% yield) of 2'-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]erythromycin A.

M.P.=136° C (hexane/ethyl acetate)

[α]_(D) ²² =-73° C. (C=1.5 mg.m/1 - dichloromethane)

Microanalysis: C₆₅ H₉₃ NO₁₄.1H₂ O; M.W.=1146.5

    ______________________________________                                                    C          H      N                                                 ______________________________________                                         Calculated, %                                                                               68.09        8.35   1.22                                          Found, %     67.99        8.40   1.14                                          ______________________________________                                    

NMR ¹³ C (CDCl₃, internal ref. T.M.S.)

Negative γ effects in 1'(-2 ppm) and 3'(=2.1 ppm) indicate the position of the ester in the 2' position.

EXAMPLE 2 Preparation of 9-0-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzoxazole carbonyl]josamycin

In a round bottom flask, under an inert atmosphere, there are dissolved 800 mg (2.3 mmoles) of 2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzoxazole carboxylic acid in 25 ml of tetrahydrofuran. The reaction mixture is then stirred for 10 hours, and the temperature is permitted to return to ambient temperature (chromatography on thin layer silica gel: methylene chloride 90%/methanol 10%). The solution is poured into 35ml of water, and then extracted with ethyl acetate. The organic phase is dried on magnesium sulfate, filtered, and then concentrated under a partial vacuum. The crude product thus obtained is chromatographed on a silica gel column (HPLC) by using as the eluant: ethyl acetate (8)/hexane (2) to result in the isolation of 250 mg (22% yield) of 9-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzoxazole carbonyl]josamycin.

[α]_(D) ²⁰ =-43 (C=1 mg.m/1, dichloromethane)

NMR ¹³ C (CDCl₃, internal ref. T.M.S) conforms to the expected spectrum.

EXAMPLE 3 Preparation of 4"-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]spiramycin

In a round bottom flask, under an inert atmosphere, there are dissolved 1.5g (3.6 mmoles) of 6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthoic acid in 35ml of anhydrous tetrahydrofuran; the solution is stirred for 1 hour and there are added 0.8ml of anhydrous pyridine, then 1.5 g (1.8 mmole) of spiramycin previously dissolved in 50 ml of tetrahydrofuran. The reaction mixture is then stirred for 10 hours and the temperature is permitted to return to ambient temperature (chromatography on thin layer silica gel: methylene chloride 90%/methanol 10%). The solution is poured into 60 ml of water, and then extracted with ethyl acetate. The organic phase is dried on magnesium sulfate, filtered, and then concentrated under a partial vacuum. The crude product thus obtained is chromatographed on a silica gel column (HPLC) by using as the eluant: ethyl acetate (7)/hexane (3) to result in the isolation of 990mg (45% yield) of 4"-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]spiramycin and a trace of a position isomer thereof.

Microanalysis: C₇₁ H₁₀₀ O₁₆ N₂.4H₂ O; M.W.=1309.6

    ______________________________________                                                          C    H                                                        ______________________________________                                         Calculated, %      64.33  8.21                                                 Found, %           64.82  7.93                                                 ______________________________________                                    

NMR ¹³ C (CDCl₃, internal ref. T.M.S.) confirms the expected spectrum.

EXAMPLE 4 Preparation of 2'-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]oleandomycin

In a round bottom flask, under an inert atmosphere, there are dissolved 1.5 g (3.6 mmoles) of 6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthoic acid in 30ml of anhydrous tetrahydrofuran; the solution is stirred for 1 hour, and there are added 0.8ml of anhydrous pyridine, then 1.4 g (1.8 mmole) of oleandomycin previously dissolved in 35 ml of tetrahydrofuran. The reaction mixture is then stirred for 10 hours and the temperature is permitted to return to ambient temperature (chromatography on thin layer silica gel: methylene chloride 90%/methanol 10%). The solution is poured into 60 ml of water and then extracted with ethyl acetate. The organic phase is dried on magnesium sulfate, filtered and then concentrated under a partial vacuum. The crude product thus obtained is chromatographed on a silica gel column (HPLC) by using as the eluant: ethyl acetate (7)/hexane (3) to result in the isolation of 1.1 g (55% yield) of 2'-O-[6-[ 3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]oleandomycin and a trace of a position isomer thereof.

M.P.=138° C. (ethyl acetate/heptane)

Microanalysis: C₆₈ H₈₇ NO₁₄.5H₂ O; M.W.=1246.5

    ______________________________________                                                    C          H      N                                                 ______________________________________                                         Calculated, %                                                                               66.2         7.93   1.13                                          Found, %     66.1         7.87   1.22                                          ______________________________________                                    

NMR ¹³ C (CDCl₃ k , internal ref. T.M.S.) conforms to the expected spectrum. The other compounds listed above can be prepared in accordance with the same operating procedures set forth in Examples 1-4.

Pharmaceutical and Cosmetic Compositions A. Gel for the topical treatment of acne

    ______________________________________                                         Hydroxypropyl cellulose  1      g                                              Butylhydroxy toluene     0.05   g                                              2'-O-[6-[3-(1-adamantyl)-4-methoxy                                                                      0.5    g                                              phenyl]-2-naphthalene carbonyl]                                                erythromycin A                                                                 Isopropanol, sufficient amount for                                                                      100    g                                              ______________________________________                                    

In this example, the active compound can be replaced by the same amount of the following compounds:

4"-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]spiramycin and

2'-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]oleandomycin.

B. Lotions for the topical treatment of acne 1.

    ______________________________________                                         Butylhydroxy toluene     0.05   g                                              2'-O-[6-[3-(1-adamantyl)-4-methoxy                                                                      1      g                                              phenyl]-2-naphthalene carbonyl]                                                erythromycin A                                                                 Triglycerides of C.sub.8 -C.sub.12 fatty acids,                                                         100    g                                              sufficient amount for                                                          ______________________________________                                    

2.

    ______________________________________                                         Butylhydroxy toluene     0.05   g                                              9-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-                                                                     1      g                                              tetramethyl-2-naphthyl)-6-                                                     benzoxazole carbonyl] josamycin                                                Isopropanol              40     g                                              Triglycerides of C.sub.8 -C.sub.12 fatty acids,                                                         100    g                                              sufficient amount for                                                          ______________________________________                                    

3.

    ______________________________________                                         Butylhydroxy toluene     0.05   g                                              2'-O-[6-[3-(1-adamantyl)-4-methoxy                                                                      1      g                                              phenyl]-2-naphthalene carbonyl]                                                oleandomycin                                                                   Isopropanol              40     g                                              Triglycerides of C.sub.8 -C.sub.12 fatty acids,                                                         100    g                                              sufficient amount for                                                          ______________________________________                                    

C. Stick for the topical treatment of acne

    ______________________________________                                         White petrolatum         52     g                                              Petrolatum oil           15     g                                              Refined paraffin         32     g                                              2'-O-[6-[3-(1-adamantyl)-4-methoxy                                                                      1      g                                              phenyl]-2-naphthalene carbonyl]                                                erythromycin A                                                                 ______________________________________                                    

In this example the active compound can be replaced by the same amount of 4"-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]spiramycin. 

What is claimed is:
 1. An aromatic ester of a macrolide or lincosamide having the formula ##STR10## wherein R represents a macrolide selected from the group consisting of:erythromycin A substituted in the 2' position, roxithromycin substituted in the 2' position, oleandomycin substituted in the 2' position, oleandomycin substituted in the 4" position, oleandomycin substituted in the 2' and 4" positions, josamycin substituted in the 9 position, josamycin substituted in the 2' position, josamycin substituted in 9 and 2' positions, spiramycin (I) substituted in the 2' position, spiramycin (I) substituted in the 4" position, spiramycin (I) substituted in the 2' and 4" positions, spiramycin (II) substituted in the 2' position, spiramycin (II) substituted in the 4" position, spiramycin (II) substituted in the 2' and 4" positions, spiramycin (III) substituted in the 2' position, spiramycin (III) substituted in the 4" position, spiramycin (III) substituted in the 2' and 4" positions, or R represents a lincosamide selected from the group consisting of:lincomycin substituted in the 3 position, clindamycin substituted in the 3 position, lincomycin substituted in the 2, 4 and 7 positions and clindamycin substituted in the 2 and 4 positions, Y represents CH or a nitrogen atom, when Y represents CH, X represents a vinylene radical, an oxygen atom, a sulfur atom or NR₁ wherein R₁ is hydrogen or methyl, when Y represents a nitrogen atom, X represents a sulfur atom, an oxygen atom or NH, Ar represents an aromatic radical having one of the following formulas: ##STR11## wherein n is 0 or 1, R₂ and R₃ represent hydrogen, linear or branched alkyl having 1-15 carbon atoms or cycloalkyl having 5-10 carbon atoms, and Z is an oxygen atom or a sulfur atom, and mixtures and salts of said esters.
 2. The ester of claim 1 selected from the group consisting of2'-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]erythromycin A, 3-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]clindamycin, 2'-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]roxithromycin, 9-O-[6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthalene carbonyl]josamycin and its 2' position isomer, 2-O-[6-(3-tert. butyl phenyl)-2-naphthalene carbonyl]erythromycin A, 2'-O-[6-[3-(1,1-dimethyl decyl)-4-methoxy phenyl]-2-naphthalene carbonyl]roxithromycia, 9-O-[6-[3-(1-adamantyl)-4-hexyloxy phenyl]-2-naphthalene carbonyl]josamycin and its 2' position isomer, 2'-O-[6-[3-(1-adamantyl)-4-decyloxy phenyl]-2-naphthalene carbonyl]spiramycin (I), (II) and (III), 2'-O-[6-[3-(1-adamantyl)-4-hydroxy phenyl]-2-naphthalene carbonyl]spiramycin (I), (II) and (III), 2'-O-[6-[4-(1-adamantylthio) phenyl]-2-naphthalene carbonyl]erythromycin A, 3-O-[6-(3-tert. butyl-4-methoxy phenyl)-2-naphthalene carbonyl]lincomycin, 3-O-[2-[3-(1-adamantyl)-4-methoxy phenyl]-5-benzimidazole carbonyl]clindamycin, 2'-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzothiazole carbonyl]erythromycin A, 2'-O-[2-[3-(1-adamantyl)-4-decyloxy phenyl]-6-benzoxazole carbonyl]roxithromycin, 9-O-[2-[3-(1-adamantyl)-4-methoxy phenyl]-6-benzo[b]furan carbonyl]josamycin and its 2' position isomer, 2'-O-[2-[3-(1-adamantyl)-4-methoxy phenyl]-6-benzo[b]thiophene carbonyl]erythromycin A, 2'-O-[2-(3-tert. butyl-4-methoxy phenyl)-6-benzo [b]furan carbonyl]oleandomycin, 2'-O-[2-[3-(1,1-dimethyl decyl)-4-methoxy phenyl]-6]benzo [b]furan-carbonyl]spiramycin (I), (II) and (III), 2'-O-[1-methyl-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-indole carbonyl]spiramycin (I), (II) and (III), 2-O-[2-(4-tert. butyl phenyl)-6-benzimidazole carbonyl]erythromycin A, 3-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzimidazole carbonyl]lincomycin, 2'-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzoxazole carbonyl]roxithromycin, 2'-O-[2-[3-(1-adamantyl)-4-methoxy phenyl]-6-benzoxazole carbonyl]erythromycin A, 9-O-[2-(4-tert. butyl phenyl)-6-benzo [b]thiophene carbonyl]josamycin and its 2 position isomer, 3-O-[2-(4-tert. butyl phenyl)-6-benzo [b]furan carbonyl]lincomycin, 2'-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzo [b]furan carbonyl]oleandomycin, 2'-O-[2-(4-tert. butyl phenyl)-6-indole carbonyl]erythromycin A, 3-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-indole carbonyl]lincomycin, 2'-O-[2-(5,6,7,8-tetrahydro-5,5 8-tetramethyl-2-naphthyl)-6-benzo [b]thiophene carbonyl]roxithromycin, 3-O-[6-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-2-naphthalene carbonyl]clindamycin, and 9-O-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-6-benzoxazole carbonyl]josamycin.
 3. A pharmaceutical or cosmetic composition for the treatment of dermatoses comprising in an anhydrous vehicle, as the active component, a pharmaceutically or cosmetically effective amount of at least one ester of claim
 1. 4. The composition of claim 3 wherein said ester is present in an amount ranging of 0.001 to 10 weight percent based on the total weight of said composition.
 5. The composition of claim 3 wherein said ester is present in an amount ranging from 0.001 to 10 weight percent based on the total weight of said composition.
 6. The composition of claim 3 wherein said anhydrous vehicle is acetone, isopropyl alcohol, triglycerides of fatty acids, C₁ -C₄ alkyl ester of a short chain acid, poly tetrahydrofuran ethers, a silicone or mixtures thereof.
 7. The composition of claim 3 which also contains a thickening agent in an amount ranging from 0.5 to 20 weight percent based on the total weight of said composition.
 8. The composition of claim 7 wherein said thickening agent is a cellulose derivative.
 9. The composition of claim 3 which also contains one or more of an antioxidant, a preservative, a perfume, a dye or another anti-acne agent. 